Our mission is to advance research for more research and
ultimately a cure for Dystonia. Click here to find out how
you can support dystonia research!
Chuck's Run for Dystonia is taking place on June 4, 2017.
Click here to see what you can do to participate.
The DMRF Canada Support Group Network provides an
opportunity for people with dystonia to come together to
support one another, raise awareness, and fund-raise. Click
here to find a support group near you!
To provide financial assistance for Canadian residents who
are living with dystonia and committed to furthering their
education. Click here to read more about eligibility
criteria and to fill out an application.
We release a bi-monthly e-newsletter on upcoming events,
research news and much more! Click here to subscribe to our
email list and receive our newsletters.
Global TV Edmonton
Jean Sharon Abbott spent nearly all of her life believing she had an incurable condition that left her feeling "trapped" in her own body -- unaware that many of her symptoms could be easily treated with a pill.
Wency Leung-The Globe and Mail. Joaquin Farias has spent the past two decades trying to understand dystonia, a confounding and sometimes debilitating syndrome believed to be the third-most-common neurological movement disorder, after essential tremor and Parkinson’s disease.